HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1603190Erstellt: 26. Oktober 2026
Hydrochloric Acid → N-(p-azidobenzenesulfonyl) N'-(3-carboxypropionyl) cystamine
https://huagongshe.com/reaction/1603190
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Cystamine Dihydrochloride | HCID 5941 | — |
| Edukt | Succinic anhydride | HCID 7922 | — |
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | N-(p-azidobenzenesulfonyl)-N'-(3-succinimidyloxycarbonyl-propionyl)cystamine | HCID 19609028 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | N-(p-azidobenzenesulfonyl) N'-(3-carboxypropionyl) cystamine | HCID 19609019 | — |
Reaktionsschritte
2.2 g of cystamine dihydrochloride were dissolved in 20 ml of water and adjusted to pH 10 with NaOH. 2.1 g of p-azidobenzenesulfochloride were suspended in the solution and the mixture was stirred at room temperature for 5 hours. The precipitated N-(p-azidobenzenesulfonyl)cystamine was reacted with 2 g of succinic anhydride and stirred overnight. The resulting solution was acidified with HCl and the product was subsequently filtered off and washed with water. The residue was dried at room temperature in a high vacuum and gave 1.53 g of N-(p-azidobenzenesulfonyl)-N'-(3-carboxypropionyl)cystamine. The IR showed bands at 3283 (amide NH), 2134 (azide), 1714 (acid carbonyl), 1650 (amide), 1589+1547 (aromatic), 1284 (COOH), 1328+1180 (arylsulfonyl), 839 (p- disubst. benzene); TLC (silica gel: conc. NH3 (EtOH=1%). Rf=0.7; m.p. 163° (dec.).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05986066 |
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| Quelldatensatz | uspto-grants-1999_11 |
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| ORD ID | ord-1098af0e084b48738a80de62db0fe224 |
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| Quellennotiz | uspto-grants-1999_11 |
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